Found 3 results
Filters: Keyword is Tubulin  [Clear All Filters]
2015
Russ JB, Borromeo MD, Kollipara RK, Bommareddy PK, Johnson JE, Kaltschmidt JA.  2015.  Misexpression of ptf1a in cortical pyramidal cells in vivo promotes an inhibitory peptidergic identity.. J Neurosci. 35(15):6028-37.
2012
Cederquist GY, Luchniak A, Tischfield MA, Peeva M, Song Y, Menezes MP, Chan W-M, Andrews C, Chew S, Jamieson RV et al..  2012.  An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation.. Hum Mol Genet. 21(26):5484-99.
2011
Tischfield MA, Cederquist GY, Gupta ML, Engle EC.  2011.  Phenotypic spectrum of the tubulin-related disorders and functional implications of disease-causing mutations.. Curr Opin Genet Dev. 21(3):286-94.